Andrew McQuillin

69.9k total citations
106 papers, 2.7k citations indexed

About

Andrew McQuillin is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Andrew McQuillin has authored 106 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 36 papers in Molecular Biology and 29 papers in Psychiatry and Mental health. Recurrent topics in Andrew McQuillin's work include Genetic Associations and Epidemiology (33 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Bipolar Disorder and Treatment (25 papers). Andrew McQuillin is often cited by papers focused on Genetic Associations and Epidemiology (33 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Bipolar Disorder and Treatment (25 papers). Andrew McQuillin collaborates with scholars based in United Kingdom, United States and Germany. Andrew McQuillin's co-authors include Hugh Gurling, David Curtis, Nicholas Bass, Sally I. Sharp, Jacob Lawrence, Gursharan Kalsi, Mie Rizig, Radhika Kandaswamy, Hannes Pétursson and Khalid Choudhury and has published in prestigious journals such as Nature Communications, PLoS ONE and American Journal of Psychiatry.

In The Last Decade

Andrew McQuillin

101 papers receiving 2.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Andrew McQuillin United Kingdom	31	1.2k	1000	772	387	309	106	2.7k
Olav B. Smeland Norway	29	1.2k 1.0×	670 0.7×	601 0.8×	264 0.7×	344 1.1×	100	2.5k
Chihiro Kakiuchi Japan	26	684 0.6×	990 1.0×	499 0.6×	265 0.7×	151 0.5×	51	2.1k
Ayman H. Fanous United States	30	1.2k 1.1×	1.1k 1.1×	702 0.9×	426 1.1×	488 1.6×	70	3.1k
Tracey L. Petryshen United States	28	1.1k 0.9×	1.2k 1.2×	555 0.7×	621 1.6×	637 2.1×	50	3.2k
Valentina Escott‐Price United Kingdom	36	1.6k 1.4×	1.2k 1.2×	793 1.0×	221 0.6×	374 1.2×	123	3.7k
Miki Bundo Japan	29	1.3k 1.1×	2.3k 2.3×	639 0.8×	471 1.2×	266 0.9×	70	3.6k
Alexander B. Niculescu United States	28	709 0.6×	1.0k 1.0×	543 0.7×	398 1.0×	252 0.8×	55	2.5k
Ru‐Band Lu Taiwan	31	519 0.4×	556 0.6×	875 1.1×	664 1.7×	291 0.9×	110	2.7k
Kazutaka Ohi Japan	31	840 0.7×	771 0.8×	903 1.2×	385 1.0×	773 2.5×	148	2.9k
Detelina Grozeva United Kingdom	21	1.2k 1.0×	857 0.9×	575 0.7×	264 0.7×	305 1.0×	40	2.2k

Countries citing papers authored by Andrew McQuillin

Since Specialization

Citations

This map shows the geographic impact of Andrew McQuillin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrew McQuillin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew McQuillin more than expected).

Fields of papers citing papers by Andrew McQuillin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew McQuillin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrew McQuillin. The network helps show where Andrew McQuillin may publish in the future.

Co-authorship network of co-authors of Andrew McQuillin

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew McQuillin. A scholar is included among the top collaborators of Andrew McQuillin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrew McQuillin. Andrew McQuillin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Levey, Daniel F., Olga Giannakopoulou, Joseph D. Deak, et al.. (2023). Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration. Nature Communications. 14(1). 6059–6059. 17 indexed citations

Gunasekara, Chathura, Eilís Hannon, Harry A. Mackay, et al.. (2021). A machine learning case–control classifier for schizophrenia based on DNA methylation in blood. Translational Psychiatry. 11(1). 412–412. 14 indexed citations

Iob, Eleonora, Tabea Schoeler, Charlotte A. M. Cecil, et al.. (2020). Identifying risk factors involved in the common versus specific liabilities to substance use: A genetically informed approach. Addiction Biology. 26(3). e12944–e12944. 8 indexed citations

Grigoroiu‐Serbânescu, Maria, Giovanni Giaroli, Johan H. Thygesen, et al.. (2019). Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD. Journal of Affective Disorders. 265. 651–659. 13 indexed citations

Fiorentino, Alessia, Sally I. Sharp, Niamh L. O’Brien, et al.. (2017). Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. Annals of Human Genetics. 82(2). 88–92. 16 indexed citations

Leonenko, Ganna, Alexander Richards, James Walters, et al.. (2017). Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(7). 724–731. 16 indexed citations

Atkinson, Stephen J., et al.. (2016). OC-031 A Genome-Wide Association Study Identifies PNPLA3 and SLC38A4 as Risk Loci for Alcoholic Hepatitis. A19.1–A19. 1 indexed citations

Kandaswamy, Radhika, Andrew McQuillin, David Curtis, & Hugh Gurling. (2014). Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(4). 365–372. 32 indexed citations

Giaroli, Giovanni, et al.. (2014). Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: A systematic review of literature and meta-analysis. Schizophrenia Research. 159(2-3). 340–346. 33 indexed citations

10.

Lydall, Gregory, Nicholas Bass, Andrew McQuillin, et al.. (2011). Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder. Psychiatric Genetics. 21(6). 294–306. 51 indexed citations

11.

Curtis, David, Andrew McQuillin, Nicholas Bass, et al.. (2010). Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. Psychiatric Genetics. 21(1). 1–4. 58 indexed citations

12.

Sharp, Sally I., Andrew McQuillin, & Hugh Gurling. (2009). Genetics of attention-deficit hyperactivity disorder (ADHD). Neuropharmacology. 57(7-8). 590–600. 99 indexed citations

13.

Perlis, Roy H., Jordan W. Smoller, Manuel A. R. Ferreira, et al.. (2009). A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder. American Journal of Psychiatry. 166(6). 718–725. 105 indexed citations

14.

Datta, Susmita, Andrew McQuillin, Mie Rizig, et al.. (2008). A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular Psychiatry. 15(6). 615–628. 45 indexed citations

15.

Kalsi, Gursharan, Andrew McQuillin, Birte Degn, et al.. (2006). Identification of the Slynar Gene (AY070435) and Related Brain Expressed Sequences as a Candidate Gene for Susceptibility to Affective Disorders Through Allelic and Haplotypic Association With Bipolar Disorder on Chromosome 12q24. American Journal of Psychiatry. 163(10). 1767–1776. 11 indexed citations

16.

Guerrini, Irene, et al.. (2005). Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2.. BMC Genetics. 6(1). 11–11. 32 indexed citations

17.

McQuillin, Andrew, Gursharan Kalsi, Soraya Mayet, et al.. (2002). A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia. European Journal of Human Genetics. 10(8). 491–494. 13 indexed citations

18.

Gurling, Hugh, David Curtis, G. Kalsi, et al.. (2000). Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 96(4). 1 indexed citations

19.

McQuillin, Andrew, et al.. (1999). Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder. Psychological Medicine. 29(6). 1449–1454. 8 indexed citations

20.

Hayes, R. J., Vini Pereira, Andrew McQuillin, & K. W. Buck. (1994). Localization of Functional Regions of the Cucumber Mosaic Virus RNA Replicase Using Monoclonal and Polyclonal Antibodies. Journal of General Virology. 75(11). 3177–3184. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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